Reaction model for kinetic of cobalt dissolution in carbonate/bicarbonate media
被引:25
作者:
Calderon, J. A.
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Univ Antioquia, Corros & Protect Grp, Medellin, ColombiaPEMM COPPE UFRJ, Lab Corrosao Prof Manoel Castro, BR-2194597 Rio De Janeiro, Brazil
Calderon, J. A.
[2
]
Barcia, O. E.
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PEMM COPPE UFRJ, Lab Corrosao Prof Manoel Castro, BR-2194597 Rio De Janeiro, BrazilPEMM COPPE UFRJ, Lab Corrosao Prof Manoel Castro, BR-2194597 Rio De Janeiro, Brazil
Barcia, O. E.
[1
]
Mattos, O. R.
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PEMM COPPE UFRJ, Lab Corrosao Prof Manoel Castro, BR-2194597 Rio De Janeiro, BrazilPEMM COPPE UFRJ, Lab Corrosao Prof Manoel Castro, BR-2194597 Rio De Janeiro, Brazil
Mattos, O. R.
[1
]
机构:
[1] PEMM COPPE UFRJ, Lab Corrosao Prof Manoel Castro, BR-2194597 Rio De Janeiro, Brazil
Cobalt dissolution in a carbonate/bicarbonate media was studied in order to elucidate the kinetic of the metal corrosion processes. Steady-state polarization and electrochemical impedance measurements were carried out during the active metal dissolution at different electrode rotation speeds. A reaction mechanism is presented in order to explain the metal dissolution: cobalt electrodissolution starts with the formation of intermediate (CoHCO3)(ads) on the electrode surface, followed by the simultaneous formation of a Co(CO3)(2)(2-) complex and the formation of a CoO film. Mass transport is characterised by diffusion of the Co(CO3)(2)(2-) complex away from the electrode. The reaction model was validated by an accurate simulation of the experimental steady-state polarisation and impedance measurements. (C) 2008 Elsevier Ltd. All rights reserved.